Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 7 (of 7 Records)

Query Trace: Disease and SMUG1[original query]
Germline whole exome sequencing and large-scale replication identifies FANCM as a likely high grade serous ovarian cancer susceptibility gene.
Oncotarget 2017 (31): 50930-50940.
Dicks Ed, Song Honglin, Ramus Susan J, Oudenhove Elke Van, Tyrer Jonathan P, Intermaggio Maria P, Kar Siddhartha, Harrington Patricia, Bowtell David D, Group Aocs Study, Cicek Mine S, Cunningham Julie M, Fridley Brooke L, Alsop Jennifer, Jimenez-Linan Mercedes, Piskorz Anna, Goranova Teodora, Kent Emma, Siddiqui Nadeem, Paul James, Crawford Robin, Poblete Samantha, Lele Shashi, Sucheston-Campbell Lara, Moysich Kirsten B, Sieh Weiva, McGuire Valerie, Lester Jenny, Odunsi Kunle, Whittemore Alice S, Bogdanova Natalia, Dürst Matthias, Hillemanns Peter, Karlan Beth Y, Gentry-Maharaj Aleksandra, Menon Usha, Tischkowitz Marc, Levine Douglas, Brenton James D, Dörk Thilo, Goode Ellen L, Gayther Simon A, Pharoah D P Pa
Association of the DNA repair SMUG1 rs3087404 polymorphism and its interaction with high sensitivity C-reactive protein for age-related macular degeneration in Iranian patients.
Ophthalmic genetics 2017 Jan 1-6.
Bonyadi Mortaza, Mehdizadeh Faride, Jabbarpoor Bonyadi Mohammad Hossein, Soheilian Masoud, Javadzadeh Alireza, Yaseri Meh
Single-nucleotide polymorphisms of uracil-processing genes affect the occurrence and the onset of recurrent depressive disorder.
PeerJ 2018 6 e5116.
Czarny Piotr, Wigner Paulina, Strycharz Justyna, Watala Cezary, Swiderska Ewa, Synowiec Ewelina, Galecki Piotr, Talarowska Monika, Szemraj Janusz, Su Kuan-Pin, Sliwinski Toma
Defective repair capacity of variant proteins of the DNA glycosylase NTHL1 for 5-hydroxyuracil, an oxidation product of cytosine.
Free radical biology & medicine 2018 12 131 264-273.
Shinmura Kazuya, Kato Hisami, Kawanishi Yuichi, Goto Masanori, Tao Hong, Yoshimura Katsuhiro, Nakamura Satoki, Misawa Kiyoshi, Sugimura Haruhi
Genetic variations in 3'UTRs of SMUG1 and NEIL2 genes modulate breast cancer risk, survival and therapy response.
Mutagenesis 2021 6 36 (4): 269-279.
Cumova Andrea, Vymetalkova Veronika, Opattova Alena, Bouskova Veronika, Pardini Barbara, Kopeckova Katerina, Kozevnikovova Renata, Lickova Katerina, Ambrus Miloslav, Vodickova Ludmila, Naccarati Alessio, Soucek Pavel, Vodicka Pav
Associations of DNA Base Excision Repair and Antioxidant Enzyme Genetic Risk Scores with Biomarker of Systemic Inflammation.
Frontiers in aging 2022 11 3 897907.
Mao Ziling, Gray Abigail L H, Gross Myron D, Thyagarajan Bharat, Bostick Roberd
Interaction of base excision repair gene polymorphism and estrogen-DNA adducts in breast cancer risk among East Asian women.
Breast cancer research and treatment 2024 7 .
Hsing-Wu Chen, Wen-Hung Kuo, Yen-Shen Lu, I-Chun Chen, Fu-Chang Hu, Ming-Yang Wang, Muhammad Zahid, Eleanor G Rogan, Ann-Lii Cheng, Ching-Hung L
TOP